Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
  • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
  • A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

Definitions

• the present invention relates to new herbicidal compositions, particularly to synergistic combinations comprising certain amidothionophosphoric acid ester compounds and a certain urea compound.
• the invention provides a herbicidal composition containing as active ingredients
• R 1 and R 2 are alkyl of from 1 to 6, preferably 1 to 4, carbon atoms,
• R 3 is hydrogen or alkyl of from 1 to 6, preferably 1 to 4, carbon atoms and
• amidothionophosphoric acid ester type compound of the foregoing formula (I) is a germination and growth inhibiting type of herbicide, which is effective against field weeds before their germination.
• the urea derivative of formula (II), which is already known from U.S. Pat. No. 2,756,135, is a herbicide of the absorption and translocating type.
• This compound has the action of either inhibiting germination or causing the weeds to wither by impeding the photosynthesis reaction.
• This compound is usually applied at the rate of 200 to 300 grams per 10 ares, and while it possesses a relatively broad herbicidal spectrum with respect to the broadleaved field weeds, its effectiveness in controlling plants that are in the growing stage is poor, and especially it has the shortcoming that its effectiveness in controlling gramineous weeds is low.
• the mixed herbicide of the invention is especially effective as a soil treating agent, it can also be used as a stem and leaf treating agent. And since certain and lasting herbicidal effects are obtained against both gramineous and broad-leaved weeds, this herbicide is helpful in saving time and labor in farming.
• the mixed herbicide of the invention can be applied in amounts of 50 - 200 grams per 10 ares (in the case of the compound of formula (I)) and of 50 - 200 grams per 10 ares (in the case of the compound of formula (II)), and this is very desirable from the standpoint of agricultural economy.
• alkyl groups R 1 , R 2 and R 3 include methyl, ethyl, n- or iso-propyl, and n-, iso-, sec.- or tert.-butyl.
• the mixture of active compounds according to the present invention can be converted into the usual formulations, such as solutions, emulsions, suspensions, powders, pastes and granulates. These may be produced in known manner, for example by mixing the active compounds with extenders, that is, liquid or solid or liquefied gaseous diluents or carriers, optionally with the use of surface-active agents, that is, emulsifying agents and/or dispersing agents, and/or foam-forming agents.
• extenders that is, liquid or solid or liquefied gaseous diluents or carriers
• surface-active agents that is, emulsifying agents and/or dispersing agents, and/or foam-forming agents.
• organic solvents can, for example, also be used as auxiliary solvents.
• liquid diluents or carriers there are preferably used aromatic hydrocarbons, such as xylenes, toluene, benzene or alkyl naphthalenes, chlorinated aromatic or aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example mineral oil fractions, alcohols, such as butanol or glycol as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, or strongly polar solvents, such as dimethyl formamide, dimethyl sulfoxide or acetonitrile, as well as water.
• aromatic hydrocarbons such as xylenes, toluene, benzene or alkyl naphthalenes
• liquefied gaseous diluents or carriers liquids which would be gaseous at normal temperatures and pressures, e.g. aerosol propellants, such as halogenated hydrocarbons, e.g. freon.
• ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, or ground synthetic minerals, such as highly-dispersed silicic acid, alumina or silicates.
• emulsifying and foam-forming agents include non-ionic and anionic emulsifiers, such as polyoxyethylene-fatty acid esters, polyoxyethylene-fatty acid esters, polyoxyethylene-fatty alcohol ethers, for example alkylarylpolyglycol ethers, alkyl sulfonates, alkyl sulfates and aryl sulfonates as well as albumin hydrolyzation products; and preferred examples of dispersing agents include lignin, sulfite waste liquors and methyl cellulose.
• non-ionic and anionic emulsifiers such as polyoxyethylene-fatty acid esters, polyoxyethylene-fatty acid esters, polyoxyethylene-fatty alcohol ethers, for example alkylarylpolyglycol ethers, alkyl sulfonates, alkyl sulfates and aryl sulfonates as well as albumin hydrolyzation products
• dispersing agents include lignin, sulfite waste liquor
• the mixture of compounds of the present invention can be used together with other agricultural chemicals, for example insecticides, fungicides, miticides, nematocides, antiviral agents, other herbicides, plant growth regulators, fertilizers, and attractants; including for example organic phosphoric ester type compounds, carbamate type compounds, dithio (or thiol) carbamate type compounds, organic chlorine type compounds, dinitro type compounds, organic sulfur or metal type compounds, antibiotics, substituted diphenyl ether type compounds, urea type compounds and triazine type compounds.
• other agricultural chemicals for example insecticides, fungicides, miticides, nematocides, antiviral agents, other herbicides, plant growth regulators, fertilizers, and attractants
• organic phosphoric ester type compounds including for example organic phosphoric ester type compounds, carbamate type compounds, dithio (or thiol) carbamate type compounds, organic chlorine type compounds, dinitro type compounds, organic sulfur or metal type compounds, antibiotics, substituted di
• the active compound mixture can be used as such or in the form of its formulations or the use forms prepared therefrom, such as ready to use solutions, emulsifiable concentrates, emulsions, foams, suspensions, spraying powders, pastes, soluble powders, dusting agents and granules. They may be applied in customary manner, for example by squirting, spraying, atomizing, dusting, sprinkling, fumigating, gassing, watering, dressing or encrusting.
• the formulations in general contain 0.1 - 95% by weight, and preferably 0.5 - 90% by weight, of total active ingredients.
• the total active compound concentrations in the ready-to-use preparations may for example be 0.0001 - 20% by weight, and preferably 0.005 to 10% by weight.
• the content of active ingredients can be suitably varied depending upon the form of the preparation, the method of its application, the purpose, the season, the place and the conditions of weed infestation.
• the active compound mixture can be used in the ultra-low-volume (ULV) method, where it is possible to apply formulations of up to 95% strength or even 100% strength.
• UUV ultra-low-volume
• the active compound mixture is generally applied to an area of agriculture in an amount of 50 - 400 grams, preferably 150 - 350 grams, of total active ingredients per 10 ares. However, in special cases the rate of application may have to be either more or less than the foregoing range.
• the invention also provides a method of combating weeds which comprises applying to the weeds or a weed habitat a composition according to the invention.
• the invention also provides means of yielding crops protected from damage by weeds by being grown in areas in which, immediately prior to and/or during the time of the growing, a composition according to the invention was applied. It will be seen that the usual methods of providing a harvested crop may be improved by the present invention.
• compositions according to the invention are illustrated by the following Examples.
• Carrier Five parts by weight of acetone
• Emulsifier One part by weight of benzyloxypolyglycol ether.
• the preparation of the active compounds was obtained as an emulsifiable concentrate by mixing one part by weight of the active compound mixture with the foregoing carrier and emulsifier in the amounts indicated.
• the prescribed concentrate in which the chemical was to be used was obtained by diluting the foregoing preparation with water.
• the mixed preparation of the invention was used in the form of an emulsifiable concentrate to treat the surface of the soil by spraying it thereon at the rate of 10 milliliters per square meter after diluting the emulsifiable concentrate to the desired chemical concentration with water.
• the weed controlling effectiveness and phytotoxicity to the crops were evaluated on a scale of 0 - 5 shown below. The results obtained are shown in Table 2, the ratings being the average value of two replicates of the test.
• a vessel 30 centimeters in length, 20 centimeters in width and 12 centimeters in depth was filled with black volcanic ash soil, after which the seeds of the weeds barnyard grass, Digitaria ciliaris, Cyperus microiria, Amaranthus blitum, Polygonum blumei, purslane, goosefoot, chickweed and kew-weed, were seeded in rows and lightly covered with soil.
• the same vessel were also transplanted onion plants of the 3-leaf stage.
• Example A the mixed preparation of the invention was used as in Example A in the form of an emulsifiable concentrate to treat the plants by spraying the emulsion onto the leaves of the plants at the rate of 100 milliliters per square meter after diluting it to the desired concentration with water.
• the weed controlling effectiveness and the selectivity with respect to onion were investigated in accordance with the same criteria as in Example A, the ratings being the average value of two replicates of the test.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Pest Control & Pesticides (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Dentistry (AREA)
• General Health & Medical Sciences (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=13985955

Family Applications (1)

Country Status (22)

Families Citing this family (2)

Citations (7)

• 1973
  • 1973-08-13 JP JP48089986A patent/JPS5040755A/ja active Pending
• 1974
  • 1974-08-06 US US05/495,174 patent/US3996039A/en not_active Expired - Lifetime
  • 1974-08-09 AT AT654074A patent/AT335795B/de not_active IP Right Cessation
  • 1974-08-09 DE DE2438291A patent/DE2438291A1/de active Pending
  • 1974-08-09 DD DD180426A patent/DD114492A5/xx unknown
  • 1974-08-09 IL IL45444A patent/IL45444A/en unknown
  • 1974-08-09 SU SU2052476A patent/SU530628A3/ru active
  • 1974-08-09 CH CH1090274A patent/CH588806A5/xx not_active IP Right Cessation
  • 1974-08-12 LU LU70715A patent/LU70715A1/xx unknown
  • 1974-08-12 GB GB3543274A patent/GB1427123A/en not_active Expired
  • 1974-08-12 DK DK428574AA patent/DK134541B/da unknown
  • 1974-08-12 IE IE1685/74A patent/IE39665B1/xx unknown
  • 1974-08-12 AU AU72256/74A patent/AU7225674A/en not_active Expired
  • 1974-08-12 ES ES429194A patent/ES429194A1/es not_active Expired
  • 1974-08-12 ZA ZA00745143A patent/ZA745143B/xx unknown
  • 1974-08-12 PL PL1974173416A patent/PL91498B1/pl unknown
  • 1974-08-12 TR TR18058A patent/TR18058A/xx unknown
  • 1974-08-12 BE BE147510A patent/BE818739A/xx unknown
  • 1974-08-13 HU HUBA3128A patent/HU169964B/hu unknown
  • 1974-08-13 NL NL7410846A patent/NL7410846A/xx unknown
  • 1974-08-13 FR FR7428060A patent/FR2240689A1/fr not_active Withdrawn
  • 1974-08-13 BR BR6650/74A patent/BR7406650D0/pt unknown

Patent Citations (7)

Also Published As

Similar Documents